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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305182Generated: November 1, 2026

Allyltributylstannane → 5-Allyl-3-(1-boc-2-(s)-azetidinylmethoxy)-6-chloropyridine

https://huagongshe.com/reaction/2305182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyltributylstannaneHCID 90628—
Reactant3-(1-BOC-2-(S)-azetidinylmethoxy)-5-bromo-6-chloropyridineHCID 22872667—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTolueneHCID 1140—
Product5-Allyl-3-(1-boc-2-(s)-azetidinylmethoxy)-6-chloropyridineHCID 2296188483.5%

Reaction Steps

3-(1-BOC-2-(S)-Azetidinylmethoxy)-5-bromo-6-chloropyridine (1.0 g, 2.65 mmol) in toluene (10 mL) was added tetrakis(triphenylphosphine) palladium (100 mg) and allyltributyltin (0.99 mL, 3.18 mmol). The mixture was stirred and refluxed for two days. Solvent was evaporated and the residue was chromatographed (silica gel; hexane/EtOAc, 5:1 to 1:1) to afford an oil (750 mg, 83%): 1H NMR (CDCl3, 300 MHz) δ 1.42 (s, 9H), 2.20-2.40 (m, 2H), 3.43 (d, 2H, J=6.5 Hz), 3.88 (t, 2H, J=7.0 Hz), 4.12 (m, 1H), 4.30 (m, 1H), 4.50 (m, 1H), 5.10-5.20 (m, 2H), 5.92 (m, 1H), 7.18 (d, J=3.0 Hz), 7.98 (d, 1H, J=3.0 Hz); MS (CI/NH3) m/z 339 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06437138B1
Source datasetuspto-grants-2002_08
ORD IDord-fa8c3028abce40c8b6b47b9bcaad97ef
Source noteuspto-grants-2002_08